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Catalyst compositions and methods of preparing them

a catalyst and composition technology, applied in the field of additive compositions, can solve the problems of short application time window after the components, the inability to improve the reaction rate by adding additional catalysts, and the use of catalysts

Active Publication Date: 2015-05-14
PPG IND OHIO INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There can be drawbacks to the use of catalysts.
Unfortunately, often the catalyst levels required to provide acceptably fast cure rates and final product properties typically result in a short application time window after the components are mixed.
Further improvements in reaction rate by adding additional catalyst are precluded because the pot life of the resulting compositions will be even shorter.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0064]An acrylic macromonomer was prepared in a 300 ml continuous stir tank reactor (CSTR) system from the following ingredients:

IngredientWt. in gButyl acrylate2406.4Lauryl methacrylate1002.6Butyl methacrylate601.5Di-t-amyl peroxide20.05

[0065]The CSTR was charged with 300 mL of 2-butoxyethanol. The above ingredients were weighed and stirred for 15 minutes at an agitation rate sufficient to provide good mixing, then charged to a feed tank while the reactor system was heating up to the reaction temperature (235° C.). When the system was at temperature, the monomer / initiator charge to the reactor was begun at a rate of 60 mL / min. Collection of the resulting acrylic macromonomer was begun 18 minutes after the feed was begun (3.6 CSTR residence times, a time sufficient to clear the 2-butoxyethanol charge from the system), and continued for 60 minutes. A reactor temperature of 235° C. and a pressure of 450-460 psig were maintained throughout the polymerization. The resulting material was...

example 2

[0066]An acrylic macromonomer co-polymer was prepared from the following ingredients:

IngredientWt. in gCharge 1Acrylic macromonomer of Ex. 11000.0Dipropylene glycol monomethyl ether550.0Propylene glycol monomethyl ether550.0Charge 2LUPEROX 7M501300.0Dipropylene glycol monomethyl ether50.0Propylene glycol monomethyl ether50.0Charge 3Acrylic acid400.0Styrene1500.0Ethyl acrylate2100.0Charge 4Dipropylene glycol monomethyl ether25.0Propylene glycol monomethyl ether25.0Charge 5Dipropylene glycol monomethyl ether25.0Propylene glycol monomethyl ether25.0Charge 6Luperox 7M5050.0Dipropylene glycol monomethyl ether12.5Propylene glycol monomethyl ether12.5Charge 7Dipropylene glycol monomethyl ether25.0Propylene glycol monomethyl ether25.0

[0067]1 t-butyl peroxyacetate, 50% solution in OMS, available from Arkema, Inc.

[0068]Charge 1 was added to a reactor equipped with a stirrer, thermocouple, and condenser, and N2 inlet. An N2 blanket was applied and the reaction mixture was heated to reflux. Cha...

example 2a

[0069]An acrylic macromonomer co-polymer was prepared from the following ingredients:

IngredientWt. in gCharge 1Acrylic macromonomer of Ex. 1200.0Dipropylene glycol monomethyl ether140.0Charge 2LUPEROX 7M50160.0Dipropylene glycol monomethyl ether20.0Charge 3Acrylic acid80.0Styrene300.0Ethyl acrylate420.0Charge 4Dipropylene glycol monomethyl ether10.0Charge 5Dipropylene glycol monomethyl ether10.0Charge 6Luperox 7M5010.0Dipropylene glycol monomethyl ether5.0Charge 7Dipropylene glycol monomethyl ether5.0

[0070]Charge 1 was added to a reactor equipped with a stirrer, thermocouple, and condenser, and N2 inlet. An N2 blanket was applied and the reaction mixture was heated to reflux. Charge 2 was added over 135 minutes; 5 minutes after Charge 2 was begun, Charge 3 was begun over 120 minutes. Charges 4 and 5 were then added as rinses for Charges 3 and 2 respectively upon completion. After the addition of Charge 5, the reaction mixture was held at temperature for 60 minutes. Charge 6 was then...

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Abstract

A catalyst composition is provided. The composition comprises at least 30 percent by weight of a catalyst compound based on the total weight of solids in the catalyst composition; and a polymer prepared from ethylenically unsaturated monomers. The polymer either (i) has a backbone derived from substantially hydrophilic monomers and / or monomers containing groups that may be rendered substantially hydrophilic after polymerization, and a plurality of side chains along the backbone derived from substantially hydrophobic monomers, or (ii) has a backbone derived from substantially hydrophobic monomers and a plurality of side chains along the backbone derived from substantially hydrophilic monomers and / or monomers containing groups that may be rendered substantially hydrophilic after polymerization. The catalyst compound is contained within or encapsulated by the polymer. Methods of preparing the catalyst composition and curable compositions containing the catalyst composition are also provided.

Description

FIELD OF THE INVENTION[0001]The present invention is directed to additive compositions, in particular, catalyst compositions and methods of preparing them.BACKGROUND OF THE INVENTION[0002]Catalysis is a change in the rate of a chemical reaction due to the participation of a material called a catalyst. Catalysts that speed the reaction are called positive catalysts. Catalysts that slow the reaction are called negative catalysts, or inhibitors. Unlike reactants, a catalyst is not consumed by the reaction itself.[0003]A catalyst works by providing an alternative reaction pathway to the reaction product. The rate of the reaction is increased when this alternative route has a lower activation energy than the reaction route not mediated by the catalyst. Catalysts can also enable reactions that would otherwise be blocked or slowed by a kinetic barrier. The catalyst may increase reaction rate or selectivity, or enable the reaction to proceed at lower temperatures than would otherwise be pos...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C09D201/00
CPCC09D201/00C09D175/04C08F220/1802C08F212/08C08F220/1804C08F220/1812C08F220/06
Inventor MORAVEK, SCOTTSCHWARTZMILLER, DAVINABARANCYK, STEVEN V.FENN, DAVID
Owner PPG IND OHIO INC